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Long-term NMDAR antagonism correlates reduced astrocytic glutamate uptake with anxiety-like phenotype

Overview of attention for article published in Frontiers in Cellular Neuroscience, June 2015
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Title
Long-term NMDAR antagonism correlates reduced astrocytic glutamate uptake with anxiety-like phenotype
Published in
Frontiers in Cellular Neuroscience, June 2015
DOI 10.3389/fncel.2015.00219
Pubmed ID
Authors

Eduardo R. Zimmer, Vitor R. Torrez, Eduardo Kalinine, Marina C. Augustin, Kamila C. Zenki, Roberto F. Almeida, Gisele Hansel, Alexandre P. Muller, Diogo O. Souza, Rodrigo Machado-Vieira, Luis V. Portela

Abstract

The role of glutamate N-methyl-D-aspartate receptor (NMDAR) hypofunction has been extensively studied in schizophrenia; however, less is known about its role in anxiety disorders. Recently, it was demonstrated that astrocytic GLT-1 blockade leads to an anxiety-like phenotype. Although astrocytes are capable of modulating NMDAR activity through glutamate uptake transporters, the relationship between astrocytic glutamate uptake and the development of an anxiety phenotype remains poorly explored. Here, we aimed to investigative whether long-term antagonism of NMDAR impacts anxiety-related behaviors and astrocytic glutamate uptake. Memantine, an NMDAR antagonist, was administered daily for 24 days to healthy adult CF-1 mice by oral gavage at doses of 5, 10, or 20 mg/kg. The mice were submitted to a sequential battery of behavioral tests (open field, light-dark box and elevated plus-maze tests). We then evaluated glutamate uptake activity and the immunocontents of glutamate transporters in the frontoparietal cortex and hippocampus. Our results demonstrated that long-term administration of memantine induces anxiety-like behavior in mice in the light-dark box and elevated plus-maze paradigms. Additionally, the administration of memantine decreased glutamate uptake activity in both the frontoparietal cortex and hippocampus without altering the immunocontent of either GLT-1 or GLAST. Remarkably, the memantine-induced reduction in glutamate uptake was correlated with enhancement of an anxiety-like phenotype. In conclusion, long-term NMDAR antagonism with memantine induces anxiety-like behavior that is associated with reduced glutamate uptake activity but that is not dependent on GLT-1 or GLAST protein expression. Our study suggests that NMDAR and glutamate uptake hypofunction may contribute to the development of conditions that fall within the category of anxiety disorders.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 67 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Canada 1 1%
Unknown 66 99%

Demographic breakdown

Readers by professional status Count As %
Researcher 9 13%
Student > Ph. D. Student 7 10%
Professor 5 7%
Student > Bachelor 4 6%
Student > Doctoral Student 4 6%
Other 11 16%
Unknown 27 40%
Readers by discipline Count As %
Neuroscience 14 21%
Agricultural and Biological Sciences 8 12%
Psychology 5 7%
Medicine and Dentistry 5 7%
Biochemistry, Genetics and Molecular Biology 2 3%
Other 3 4%
Unknown 30 45%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 26 May 2015.
All research outputs
#20,274,720
of 22,807,037 outputs
Outputs from Frontiers in Cellular Neuroscience
#3,569
of 4,241 outputs
Outputs of similar age
#223,194
of 267,099 outputs
Outputs of similar age from Frontiers in Cellular Neuroscience
#102
of 118 outputs
Altmetric has tracked 22,807,037 research outputs across all sources so far. This one is in the 1st percentile – i.e., 1% of other outputs scored the same or lower than it.
So far Altmetric has tracked 4,241 research outputs from this source. They typically receive a little more attention than average, with a mean Attention Score of 6.2. This one is in the 1st percentile – i.e., 1% of its peers scored the same or lower than it.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 267,099 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 1st percentile – i.e., 1% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 118 others from the same source and published within six weeks on either side of this one. This one is in the 1st percentile – i.e., 1% of its contemporaries scored the same or lower than it.